Draeger, Inc. recalled 188 units of the Vapor 3000 anesthetic vaporizer on November 24, 2025. The devices contained impurities in a component not delivered within specification. Healthcare providers and patients must stop using the devices immediately.
A certain component of affected devices was not delivered within specification and contained impurities.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Draeger, Inc. or your healthcare provider for instructions. Notification method: Letter
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The Draeger Vapor 3000 is an unheated, calibrated anesthetic vaporizer used in medical settings for delivering anesthetic gases to patients. Healthcare providers typically use this device during surgical procedures to ensure patient safety.
The vaporizer is recalled due to a component that contains impurities and does not meet the required specifications, which may compromise patient safety during anesthesia delivery.
This recall is not part of a broader industry pattern.
The recall may cause disruption in medical settings that rely on the Draeger Vapor 3000 for anesthetic administration, potentially delaying procedures and impacting patient care.
The model number and serial numbers are usually located on the device's label or in the product documentation.
Expect a refund or replacement process to take approximately 4-6 weeks.
Keep records of your purchase, correspondence with Draeger, and any incident reports related to the device.
The recall affects the Draeger Vapor 3000 anesthetic vaporizer, model number M36500. These devices were distributed worldwide, including across 13 U.S. states such as California and New York. The quantity recalled is 188 units.
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